rs1050388

Orientation

minus

Stabilized

minus

Geno	Mag	Summary
(G;G)	0	common in clinvar

Make rs1050388(A;A)

Make rs1050388(A;G)

Reference

GRCh38 38.1/141

Chromosome

6

Position

31356729

Gene	HLA-B, MIR6891

is a	snp
is	mentioned by
dbSNP	rs1050388
dbSNP (classic)	rs1050388
ClinGen	rs1050388
ebi	rs1050388
HLI	rs1050388
Exac	rs1050388
Gnomad	rs1050388
Varsome	rs1050388
LitVar	rs1050388
Map	rs1050388
PheGenI	rs1050388
Biobank	rs1050388
1000 genomes	rs1050388
hgdp	rs1050388
ensembl	rs1050388
geneview	rs1050388
scholar	rs1050388
google	rs1050388
pharmgkb	rs1050388
gwascentral	rs1050388
openSNP	rs1050388
23andMe	rs1050388
SNPshot	rs1050388
SNPdbe	rs1050388
MSV3d	rs1050388
GWAS Ctlg	rs1050388

GMAF

0.2181

Max Magnitude

0

ClinVar
Risk	rs1050388(A;A) rs1050388(C;C)
Alt	rs1050388(A;A) rs1050388(C;C)
Reference	Rs1050388(G;G)
Significance	Histocompatibility
Disease
Variation	info
Gene	HLA-B
CLNDBN
Reversed	1
HGVS	NC_000006.11:g.31324506C>G; NC_000006.11:g.31324506C>T
CLNSRC
CLNACC